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-14% CALCIGEN D Citro 600 mg/400 I.E. chewing tablets, 50 pcs

CALCIGEN D Citro 600 mg/400 I.E. chewing tablets, 50 pcs

CALCIGEN D Citro 600 mg/400 I.E. Kautabletten

Manufacturers: MEDA Pharma GmbH & Co.KG

PZN: 01138539

Dosage: Kautabletten

Content: 50 St

Reward Points: 128

Availability: Out of stock

$19.19

$16.44

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-14% CALCIGEN D Citro 600 mg/400 I.E. chewing tablets, 50 pcs
  • CALCIGEN D Citro 600 mg/400 I.E. chewing tablets, 50 pcs
  • CALCIGEN D Citro 600 mg/400 I.E. chewing tablets, 50 pcs

Instructions for use for CALCIGEN D Citro 600 mg/400 I.E. chewing tablets, 50 pcs

Calcigen D Citro 600 mg/ 400 I.E. chewing tablets
 
Composition:
1 Chewing tablet contains 1500 mg calcium carbonate (corresponding to 600 mg calcium) and 4 mg Colecalciferol drying concentrate (corresponding to 400 I.E. vitamin D3).
Other components: xylitol, mannitol, magnesium stearate, high-disperse silicon dioxide, pre-clad cornstarch, butylhydroxytoluol (E321), medium-chain triglycerides, sucrose, gelatin, modified starch, sodium aluminum silicate, aroma substances.
 
Application areas:
Compensation for combined vitamin D and calcium deficiency in older patients. Vitamin D and calcium supplement as an addition to a specific osteoporosis treatment of patients in which a combined vitamin D and calcium deficiency was determined or in which there is a high risk of such deficiency states.

With a citrus taste

Detailed instructions for CALCIGEN D Citro 600 mg/400 I.E. chewing tablets, 50 pcs

Field of use

  • This medicine contains the two active ingredients calcium and vitamin D3. Calcium is an important part of the bones and vitamin D3 improves the intake of calcium from the intestine and installation in the bones.
  • It is used at:
    • Compensation for combined vitamin D and calcium deficiency in older patients
    • as an addition to an osteoporosis treatment in which the vitamin D and calcium levels are too low or there is a high risk of this.

Active ingredients / ingredients / ingredients

1500 mg calcium carbonate
600 mg calcium ion
4 mg Colecalciferol dry concentrate
400 Ie Colecalciferol
10 µg Colecalciferol
Butylhydroxytoluol HILDUFT (+)
Gelatine auxiliary substance (+)
Magnesium stair (Ph. EUR.) [pflanzlich] Hedge substance (+)
Corn starch, pre -clerked auxiliary substance (+)
Mannitol Hilfoff (+)
Sodium aluminum silicat auxiliary substance (+)
1.54 mg sucrose auxiliary material (+)
Silicium dioxide, high disperser auxiliary substance (+)
Strength, modified auxiliary substances (+)
Triglyceride, medium -chain auxiliary material (+)
Xylitol auxiliary substance (+)
0.47 g Total carbohydrates Hedge substance (+)
0.04 Be overall carbohydrates HILDVERSTOFT (+)
Lemon aroma hedge material (+)

Contradictions

  • The preparation must not be taken
    • if you are allergic to calcium carbonate, vitamin D or one of the other components of this medicine.
    • in the case of too high calcium concentrations in the blood (hypercalcemia) and/or increased calcium excretion in the urine (hypercalcuria)
    • if you have the prerequisites that lead to hypercalcemia and/or hypercalcuria [z. B. Überfunktion der Nebenschilddrüsen, eine Erkrankung des Knochenmarks (Myelom), ein bösartiger Knochentumor (Knochenmetastasen)]
    • if you are affected by severe renal insufficiency or kidney failure
    • if you suffer from kidney stones (nephrolithiasis) or lime deposits in the kidneys (nephrocalcinosis)
    • if you suffer from vitamin D overdosing (hypervitaminosis d).

dosage

  • Always take this medicine exactly as described or exactly after the agreement made with your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure.
  • Dosage
    • The usual dose for adults and the elderly is one tablet twice a day (e.g. one in the morning and one in the evening). Pregnant women should only take one tablet a day.
    • With long -term treatment, the calcium levels in the urine and blood must be monitored. This is particularly important if you develop kidney stones more often.
  • Application in children and adolescents
    • This preparation is not suitable for use in children and adolescents.

 

  • Duration of the application
    • The doctor decides on the duration of the treatment.

 

  • If you have taken a larger amount than you should
    • If you have taken a larger amount than you should and notice signs of an overdose, please interrupt the intake and HALif you immediately consult your doctor. Signs of overdosing can be: drying out, loss of appetite, increased thirst, nausea, vomiting, constipation, abdominal pain, muscle weakness, fatigue, mental disorders, pathologically increased urine excretion, bone pain, kidney stones.
    • Chronic overdosing can lead to vascular and organ calcification through limescale deposits.
    • In the event of considerable overdose, cardiac arrest can occur.

 

  • If you have forgotten the intake
    • Do not take the double amount if you have forgotten the prior intake.

 

  • If you cancel the intake
    • If you want to interrupt the treatment or end prematurely, please consult your doctor.

 

  • If you have any further questions about the application of this medicine, please contact your doctor or pharmacist.

Taking

 

  • The chewing tablets should be chewed and then swallowed with the help of some liquid. In exceptional cases, e.g. B. in patients with chewing problems, the tablets can also be sucked after consultation with the doctor.
  • Pregnant and breastfeeding women should take this medicine two hours before or after meals in order to avoid a possible impairment of iron absorption.

Patient information

  • Warnings and Precautions
    • Please speak to your doctor or pharmacist before taking the preparation.
    • During long -term treatment with the preparation, the calcium level in the serum and by measuring the serum creatinine, the kidney function should be checked regularly. This review is particularly important in older patients and at the same time treatment with heart glycosides (e.g. digoxin) and diuretics. Based on the results obtained, your doctor can recommend reducing your dose or even canceling the treatment. However, the dose should be reduced or the therapy is temporarily interrupted if the calcium excretion via the urine exceeds 7.5 mmol/24 hours (300 mg/24 hours).
    • Before taking this preparation, the amount of vitamin D, calcium and alkali such as B. carbonate from other sources (e.g. nutritional supplements or food). Since these products already contain vitamin D and calcium carbonate, the additional intake can lead to burnnth syndrome. BurnetSyndrome (milk alkali syndrome) is a calcium metabolic disorder with an increase in blood-calcium level. It can be triggered by absorbing very large amounts of milk and/or calcium carbonate from other sources or by excessive use of antacids (agent against stomach acidification). Therefore, an additional administration of this preparation must be carried out under strict medical control with regular checking of calcium levels in blood (calcaemia) and urine (calciurie).
    • Before taking it, you should consult with your doctor or pharmacist:
      • if you suffer from kidney stones
      • if you suffer from an illness of the immune system (sarcoidosis), since the calcium level must be checked in blood and urine
      • if your ability to move is restricted and you suffer from a reduced bone mass (osteoporosis). This can increase your blood calcium level so much that side effects can occur.
      • if you also take other vitamin D3 or calcium-containing preparations. Your blood calcium level can increase so much that side effects can occur.
      • if you suffer from a slight to moderate kidney dysfunction. With severe kidney dysfunction, you must not take this medicine.
    • Children and adolescents
      • The preparation is not suitable for use in children and adolescents.

 

  • Wateriness and ability to operate machines
    • There are no effects on the traffic and operating machines.

Pregnancy

  • If you Schwangers are or breastfeeding, or if you suspect that you are pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before taking this drug.
  • Pregnant and breastfeeding women should take this medicine two hours before or after meals in order to avoid a possible impairment of iron absorption.
  • Pregnancy
    • The preparation can be applied during pregnancy, but the daily intake should not exceed 1,500 mg calcium and 600 i.e. vitamin D. In the event of pregnancy, you may not take more than one tablet every day. Higher doses can affect the unborn child.
  • Breastfeeding
    • This preparation can be used during breastfeeding. Since calcium and vitamin D3 pass into breast milk, you must first consult your doctor whether your child already receives products that contain vitamin D3.
    •  

Hints

Read the package supplement and ask your doctor or pharmacist for risks and side effects.

Manufacturer:  MEDA Pharma GmbH & Co.KG, Benzstraße 1, 61352 Bad Homburg

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